CORONAVIRUS - ANVISA Registration 81246986875

Access comprehensive regulatory information for CORONAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81246986875 and manufactured by QUIDEL CORPORATION. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA with validity until Nov 30, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including GUANGZHOU WONDFO BIOTECH CO., LTD., Eco Diagnostica Ltda, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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81246986875
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Registration Details
ANVISA Registration Number: 81246986875
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

SOFIA® SARS ANTIGEN FIA
Risk Class III

Registration Details

81246986875

25351309316202318

21921393000146

Company Information

QUIDEL CORPORATION
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 19, 2023

30/11/2030

09/18/2025 19:00:01

SOFIA® SARS ANTIGEN FIA
Risk Class III

Registration Details

81246986875

25351309316202318

21921393000146

Dates and Status

Jun 19, 2023

30/11/2030

09/18/2025 19:00:01